Green Synthesis of a Fluorescent Natural Product

• Douglas M. Young ^[1] ; Jacob J. C. Welker ^[1] ; Kenneth M. Doxsee ^[1]
  1. [1] Department of Chemistry, University of Oregon, United States
• Localización: Journal of chemical education, ISSN 0021-9584, Vol. 88, Nº 3, 2011, págs. 319-321
• Idioma: inglés
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• Resumen

  • Synthesis of 4-methylumbelliferone via the acid-catalyzed Pechmann condensation introduces students to several types of organic reactions: transesterification, electrophilic aromatic substitution, and alcohol dehydration. Performed with a recyclable, solid catalyst and under solvent-free conditions, the experiment illustrates many of the principles of green chemistry and additionally illustrates the potential of green chemistry to yield not only safety and environmental benefits, but positive economic impacts as well. With high regioselectivity, complex yet interpretable IR and 1H NMR spectra, and unusual pH-dependent fluorescence, the synthesis of 4-methylumbelliferone provides a rich learning platform.